Varian Assoc., Inc.

Varian Assoc., Inc. — FDA 510(k) Submissions

Varian Assoc., Inc. has submitted 86 FDA 510(k) premarket notifications since 1976, of which 86 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Accelerator, Linear, Medical, Colorimeter, Photometer, Spectrophotometer For Clinical Use, System, Simulation, Radiation Therapy, Atomic Absorption Spectrophotometer, General Use, System, Applicator, Radionuclide, Remote-controlled . Use the specialty filter in the sidebar to narrow results.